The introduction of oxygen atoms into different positions of the vitamin D
side chain is described. By combining the arising 23-oxa and 25-oxa element
s with other structural modifications (19-nor, iso-19-nor, 20-methyl, 20-en
e, 20,21-cyclo) calcitriol analogs with remarkable levels of dissociation b
etween beneficial acitivities on cell growth regulation and undesired hyper
calcemia were identified. Structure-activity relations are elaborated in a
very systematic outline of the Schering drug finding program in this partic
ular class of vitamin D compounds.